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2-Pyrrolidinecarboxamide, 5-oxo-N-phenyl-, also known as Phenylsuccinimide (PSI), is an organic compound with the chemical formula C10H10N2O2. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 97-98°C. PSI is a cyclic imide derived from phenylsuccinic acid, where the carboxylic acid group is replaced by an amide group. It is widely used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactive imide functionality. Additionally, it serves as a chiral auxiliary in asymmetric synthesis and as a reagent in peptide synthesis. The compound is also known for its ability to undergo various chemical reactions, such as nucleophilic addition, making it a valuable building block in organic chemistry.

5626-54-0

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5626-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5626-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5626-54:
(6*5)+(5*6)+(4*2)+(3*6)+(2*5)+(1*4)=100
100 % 10 = 0
So 5626-54-0 is a valid CAS Registry Number.

5626-54-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-oxopyrrolidine-2-carboxanilide

1.2 Other means of identification

Product number -
Other names 5-oxo-prolin-anilide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5626-54-0 SDS

5626-54-0Relevant academic research and scientific papers

Controlled ring-opening polymerization of α-amino acid N-carboxy-anhydride by frustrated amine/borane Lewis pairs

Zhang, Hongyuan,Nie, Yanzhao,Zhi, Xinmei,Du, Haifeng,Yang, Jing

supporting information, p. 5155 - 5158 (2017/07/12)

In this communication, we presented a novel strategy to control the ROP of α-amino acid N-carboxy-anhydrides using the concept of frustrated Lewis pairs (FLPs). An FLP intermediate containing an interaction between the bulky borane Lewis acid and the amine groups of the propagation chain end is essential to accomplish the polypeptide synthesis with well-defined structures under mild conditions.

Studies on pyrrolidinones. Synthesis and reactivity of some N-protected pyroglutamic derivatives

Rigo,Erb,El Ghammarti,Gautret,Couturier

, p. 1599 - 1604 (2007/10/03)

The synthesis of pyroglutamoyl chloride N-protected by a methoxycarbonyl or a trifluoroacetyl group is described. Some aspects of the reactivity of these compounds and intermediates have been studied.

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